Tobias Geis

Homozygous dystroglycan mutation associated with a novel muscle–eye–brain disease-like phenotype with multicystic leucodystrophy

Tobias Geis, Klaus Marquard, Tanja Rödl et al. · Neurogenetics · 2013 · 79 citations

Homozygous Dystroglycan Mutation, Neurodegenerative Diseases, Mendelian Disorder +12

Serum neurofilament light chain reference database for individual application in paediatric care: a retrospective modelling and validation study

Ahmed Abdelhak, Franziska Petermeier, Pascal Benkert et al. · The Lancet Neurology · 2023 · 45 citations

Primary Care, Medicine, Pediatrics +8

Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders

Tobias Geis, Tanja Rödl, Haluk Topaloğlu et al. · Orphanet Journal of Rare Diseases · 2019 · 41 citations · Full text

LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs

Saskia M. Herbst, Christiane R. Proepper, Tobias Geis et al. · Brain and Development · 2015 · 38 citations

Antiepileptic Drugs, Medicine, Neuropharmacology +6

Tacrolimus (FK506)-induced cerebral blindness following bone marrow transplantation.

Steve Devine, Nancy J. Newman, Jerald Siegel et al. · PubMed · 1996 · 34 citations